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| Item Type: | Article |
|---|---|
| Title: | Clinical implications and dynamics of clonal hematopoiesis in anti-CD19 CAR T-cell treated patients |
| Creators Name: | Panagiota, V. and Kerschbaum, J.F. and Penack, O. and Stein, C.M. and Arends, C.M. and Koenecke, C. and Strzelecka, P.M. and Kloos, A. and Wiegand, L. and Lasch, A. and Altwasser, R. and Halik, A. and Gabdoulline, R. and Thomson, J. and Weibl, K. and Franke, G.N. and Berger, C. and Hasenkamp, J. and Ayuk, F. and Na, I.K. and Beutel, G. and Keller, U. and Bullinger, L. and Wulf, G.G. and Kröger, N. and Vucinic, V. and Heuser, M. and Damm, F. |
| Abstract: | Recent evidence revealed important interactions between clonal hematopoiesis (CH) and cellular therapies established for the treatment of hematologic malignancies. The impact of CH on safety, efficacy, and outcome of chimeric antigen receptor (CAR) T-cell therapy is currently under investigation. We analyzed 110 patients with relapsed/refractory B-cell non-Hodgkin lymphoma (n = 105) or acute lymphoblastic leukemia (ALL) (n = 5), treated with Axicabtagene-Ciloleucel (39%), Tisagenlecleucel (51%), or Brexucabtagene autoleucel (10%). Using error-corrected targeted sequencing, a high CH prevalence of 56.4% (variant allele frequency [VAF] ≥1%) at the time of CAR T-cell infusion was detected. The most frequently mutated gene was PPM1D followed by DNMT3A, TET2, ASXL1, and TP53. Variant allele frequencies were significantly lower in B and T cells compared with monocytes and granulocytes. CH did not increase the risk of CAR T-related toxicities. The incidences of cytokine release syndrome and immune effector-cell-associated neurotoxicity syndrome were similar between CH(pos) and CH(neg) patients, regardless of clone size, age, or CAR T product. Prolonged cytopenias were not associated with CH. Best overall response rates (ORRs) were numerically but not significantly higher in CH(pos) patients (ORR 76.7% versus 62.2%; P = 0.13). Furthermore, CH status did not predict progression-free survival or overall survival. Lastly, sequential analysis showed a modest VAF increase of 1.3% and acquisition of novel mutations within 100 days postinfusion. CH was frequent in large B-cell lymphoma/ALL patients receiving CAR T-cells but did not affect toxicity nor treatment response or outcome. |
| Source: | HemaSphere |
| ISSN: | 2572-9241 |
| Publisher: | Wolters Kluwer |
| Volume: | 7 |
| Number: | 10 |
| Page Range: | e957 |
| Date: | October 2023 |
| Official Publication: | https://doi.org/10.1097/hs9.0000000000000957 |
| PubMed: | View item in PubMed |
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